Patent Application
20130211076
The present invention provides a new synthesis for preparing N-(3-amino-quinoxalin-2-yl)-sulfonamides of general formula (I) and its intermediate N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formula (II). The compounds of formulae (I) and (II) are useful building blocks, in particular in the synthesis of drugs.
The present invention is related to a new synthesis for preparing N-(3-amino-quinoxalin-2-yl)-sulfonamides of general formulae (I) and (I′), and their intermediates N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formulae (II) and (II′):
R1 is selected from the group consisting of A, C3-C8-cylcoalkyl, Het, and Ar.
R2 is selected from the group consisting of Ar and Het.
Ar denotes a monocyclic or bicyclic, aromatic carbocyclic ring having 6 to 14 carbon atoms, which is unsubstituted or monosubstituted, disubstituted or trisubstituted by Hal, CF3, OCF3, NO2, CN, perfluoroalkyl, A, —OR6, —NHR6, —CORE, —CONHR6, —CON(R6)2, —NR6COR6, —NR6CO2R6, —NR6SO2A, NR6CONR′R″, —COOR6, —SO2A, —SO2NR6A, —SO2Het, —SO2NR6Het, Ar, Het, —NR6SO2NR6Het, COHet, COAr, or C3-C8-cycloalkyl.
Het denotes a monocyclic or bicyclic saturated, unsaturated or aromatic heterocyclic ring having 1 to 4 N, O and/or S atoms and/or 1 group selected from CO, SO or SO2, which is unsubstituted or monosubstituted, disubstituted or trisubstituted by Hal, CF3, OCF3, NO2, CN, perfluoroalkyl, A, —OR6, —NHR6, —CORE, —CONHR6, —CON(R6)2, —NR6COR6, —NR6CO2R6, —NR6SO2A, NR6CONR′R″, —COOR6, —SO2A, —SO2NR6A, —SO2Het, —SO2NR6Het, Ar, Het, —NR6SO2NR6Het, or C3-C8-cycloalkyl.
A is a branched or linear alkyl having 1 to 12 C-atoms, wherein one or more, preferably 1 to 7H-atoms may be replaced by Hal, Ar, Het, OR6, CN, NR6COA, CONR′R″, COOR6 or NR′R″ and wherein one or more, preferably 1 to 7 non-adjacent CH2-groups may be replaced by O, NR6 or S and/or by —CH═CH— or —C≡C— groups, or denotes cycloalkyl, cycloalken or cycloalkylalkylen having 3-7 ring C atoms wherein the cycloalkylen is optionally substituted by 1 to 3 groups selected from OR6, Hal, Ar, Het, CN, NR6COA, CONR′R″, COOR6;
R′, R″ denote independently from each other H, A, Ar, or Het,
The method employs commercially available, or easily obtainable, starting compounds.
The synthetic approaches for preparing N-(3-amino-quinoxalin-2-yl)-sulfonamides (I) are well known. Examples from the prior art reports the reaction of the 2,3-dichloro-quinoxaline (commercially available or easily obtainable from commercially available starting compounds, scheme 1) with the sulfonamide of formula (III) wherein R1 is a aryl or heteroaryl group, to give the intermediate (II) (Scheme 1, Step 1). In a second step, the intermediate N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formula (II) is converted to the N-(3-amino-quinoxalin-2-yl)-sulfonamides (I) by reaction with an amine of formula (IV) wherein R2 is a aryl or heteroaryl group (Scheme 1, Step 2).
Several documents quote the transformation of the 2,3-dichloro-quinoxaline with sulfonamides of formula (III) into N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formula (II) in the presence of carbonates as bases (e.g. K2CO3 or Cs2CO3) in polar aprotic solvents such as DMSO, DMF, NMP or DMA (References 1-9), Scheme 2.
For example, the patent application (WO 2007023186 A1, Reference 2) described the reaction of the 2,3-dichloro-quinoxaline with a compound of Formula (III) wherein R1 is a phenyl group, i.e. phenylsulfonamide, with potassium carbonate in DMA at 135° C. (80% yield). The same compound was prepared by S. V. Litvinenko et al. (Reference 7) using potassium carbonate in DMF at reflux.
A further example for the synthesis of compounds of Formula (II), wherein R1 is dichlorophenyl, can be found in WO 2005021513 A1 (Reference 4, example 10 step a, p27) In this example, cesium carbonate is used as a base for the transformation.
For the formation of N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formula (II), the above methods found in the literature described the use of carbonate bases such as potassium or cesium carbonate. These conditions may need long reaction time or higher temperature for completion. In addition, these reaction conditions may cause the formation of undesired by-products or impurities that are difficult or expensive to remove.
The present invention provides a new method for the synthesis of compounds of Formula (I), wherein step I in scheme 1 does not require the use of the carbonates as a base, but the use of alkali metal hydroxide, particularly lithium hydroxide as a base. Use of an alkali metal hydroxide improves the purity profile and the yield. In addition, use of an alkali metal hydroxide allows to have similar reaction time at lower temperature or to have decreased reaction time.
The second step (scheme 1) consisting in the transformation of compounds of Formula (II) into compounds of Formula (I) is reported in the literature (References 1, 2, 8, 9). These reports often disclosed the reaction at elevated temperature in polar solvents such as DMA, DMF, NMP, DMSO or EtOH, or alternatively, aprotic non polar solvents such as toluene or xylene. Alternative conditions are the use of acetic acid in DMA.
For example, the patent application WO 2007023186 A1, (Reference 2) described the reaction of 4-cyano-N-(3-chloro-quinoxalin-2-yl)-sulfonamides with the 3,5-dimethoxy aniline (IV) in EtOH heated at 100° C. overnight (50% yield), (scheme 4).
WO 2008127594, (Reference 8, example 373, p434) described the reaction of a compound of Formula (II) wherein R1 is phenyl with the 4-fluoro aniline in DMA at 120° C., during 25 minutes, under microwave irradiation (62% yield), (Scheme 5).
WO 2008127594, (Reference 8, example 14, p379) also described the reaction of N-(3-chloro-quinoxalin-2-yl)-sulfonamides (II) wherein R1 is a 3 nitro-phenyl with the 3,5-dimethoxy-aniline in xylene at 150° C. (70% yield), (Scheme 6).
In the formation of N-(3-amino-quinoxalin-2-yl)-sulfonamides of formula (I), the above methods found in the literature involve the heating of an amine of formula NH2R2 in different solvent without bases, or with acetic acid. These conditions may need long reaction time or higher temperature for completion. In addition, these reaction conditions may cause the formation of undesired by-products or impurities that are difficult or expensive to remove.
The present invention provides a new method requiring the use of a pyridine base, preferably the 2,6-dimethylpyridine (lutidine). The use of this base led to improved purity profile and/or improved yields. Also, these conditions allow to have similar reaction time at lower temperature or to have decreased reaction time.
The present invention provides improved conditions for the preparation of N-(3-amino-quinoxalin-2-yl)-sulfonamides of general formulae (I) and (I′), and their intermediates N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formulae (II) and (II′).
In particular, the present invention provides a new method for the first step (scheme 7) that use of alkali metal hydroxide as a base, improving the purity profile, the yield and allowing to reach excellent yields and conversions at lower temperature compared to the use of other bases such as carbonates, or allowing to reach excellent yields and conversions at the same temperature but in shorter reaction time. The preferred conditions are the ones using lithium hydroxide as the base.
In addition, the present invention provides a new method for the second step (Scheme 6) that use a pyridine base, preferably 2,6-dimethylpyridine (lutidine), improving the purity profile, the yield and allowing to reach excellent yields and conversions at lower temperature compared to the conditions described in the literature, or allowing to reach excellent yields and conversions at the same temperature but in shorter reaction time.
The alkali metal hydroxide bases used in the first step of the synthesis are preferably selected from NaOH, KOH, and LiOH.
An aprotic solvent denotes an organic solvent which does not exchange proton, or “H atom” with the products which are dissolved in it. Aprotic solvents comprises polar aprotic solvents and apolar aprotic solvents.
Examples of polar aprotic solvents are Dichloromethane (DCM), Tetrahydrofuran (THF), Ethyl acetate, Acetone, Dimethylformamide (DMF), Acetonitrile (MeCN), Dimethyl sulfoxide (DMSO), dimethylacetamide (DMA), N-methylpyrrolidone (NMP).
The crude purity of a compound e.g. compounds of Formula (II) or compounds of Formula (I), denotes the ratio of said compounds compared to the other impurities or by-products obtained in the crude mixture, before the purification step. The crude purity is preferably determined using commonly used analytical methods like HPLC (High performance liquid chromatography), GC (Gaz chromatography), GC-MS (Gaz chromatography couple with Mass spectrometry), SFC (supercritical fluid chromatography). These methods may include or not the use of internal references.
Ar preferably denotes a monocyclic or bicyclic, aromatic carbocyclic ring having 6 to 14 carbon atoms, which may be monosubstituted, disubstituted or trisubstituted by:
When a variable is present more than one time in a group, each variable independently denotes one of the values provided in its definition.
Het preferably denotes a monocyclic or fused bicyclic saturated, unsaturated or aromatic heterocyclic ring having 1 to 3 N, O and/or S atoms and/or 1 CO group, preferably 1 to 2 N, O and/or S atoms, which may be monosubstituted, disubstituted or trisubstituted by:
When Het is a fused bicyclic group, it is enough that one of the cyclic group contains 1 to 4 N, O, and/or S atom or a group selected from CO, SO or SO2. As examples Het also includes a phenyl or a saturated or unsaturated carbocyclic ring fused with saturated, unsaturated or aro-matic heterocyclic ring having 1 to 4 N, O and/or S atoms and/or 1 group selected from CO, SO or SO2, and optionally substituted with the substitutents defined in Het.
More preferably, Het denotes one of the following groups:
Preferably, the group A denotes a branched or linear alkyl having 1 to 6 C-atoms, wherein one or more, preferably 1 to 3H-atoms may be replaced by:
Preferably, the reaction is performed in DMA, DMF or DMSO.
Step 2: Then, the intermediate N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formula (II) is transformed into a compound of Formula (I) wherein R1 is as above defined by reaction with amine of formula NH2R2 where R2 is as above defined, using a pyridine base such as pyridine, methylpyridine or dimethylpyridine such as lutidine as a base. The reaction is preferably performed in a polar solvent such as such as DMA, DMF, NMP, DMSO or alcohol (EtOH, MeOH, iPrOH, n-propanol, n-butanol). The temperature of the reaction is ranging from 20° C. to 150° C. for a period from 0.5 to 48 hours (depending on the nature of the amine NH2R2 and of the intermediate (II)).
Preferably, the reaction is performed with 2,6-di-methyl-pyridine (lutidine or 2,6-lutidine) in an alcohol such as n-butanol or n-propanol.
The isolated yield of a compound or an intermediate refers to the yield of such compound or intermediate obtained after a purification step. A purification step is any step intending to remove impurities from the crude mixture after the reaction, using any purification method which is deemed proper. Examples of purification methods are chromatography, crystalisation, distillation, extraction, adsorption, evaporation, centrifugation, or fractionation.
In a first embodiment, the first step of the process of the present invention provides the compounds of Formulae (II) or (II′) in an isolated yield higher than 50%, preferably higher than 70% and most preferably higher than 80%, using an alkali metal hydroxide in a polar aprotic solvent at a temperature between 30° C. and 80° C. More preferably, compounds of Formula (II) are obtained using a polar aprotic solvent at a temperature around 50° C., in a reaction time between 10 hours and 20 hours. More preferably compounds of Formula (II) are obtained in a yield higher than 60% using an alkali metal hydroxide selected from LiOH, KOH and NaOH, preferably LiOH, at a temperature between 40° C. and 60° C., in a polar aprotic solvent selected from DMA, DMSO, NMP, DMF, preferably DMA, in a reaction time of 10 to 24 hours, preferably 15 to 20 hours.
In a second embodiment, the first step of the process of the present invention provides compounds of Formulae (II) or (II′) with a crude purity higher than 70%, using an alkali metal hydroxide in a polar aprotic solvent at a temperature of 40° C. to 60° C. Preferably the reaction time lasts between 10 to 20 hours, more preferably, between 15 to 18 hours. More preferably, the first step of the process of the present invention provides compounds of Formula (II) with a crude purity higher or equal to 80%, using an alkali metal hydroxide selected from LiOH, or KOH, in a polar aprotic solvent selected from DMA, DMSO, NMP and DMF, preferably DMA, at a temperature of 40° C. to 60° C., preferably around 50° C., with a reaction time of 15 to 20 hours, preferably around 16 hours.
In a third embodiment, the first step of the process of the present invention provides compounds of Formulae (II) or (II′) with a crude purity higher than 80%, in a time shorter than 24 hours at a temperature lower than 90° C.
In a fourth embodiment, the first step of the process of the present invention provides compounds of Formulae (II) or (II′) with a crude purity higher than 70%, in a time shorter than 5 hours, preferably shorter than 3 hours, more preferably in around 1 hour, at a temperature lower or equal to 100° C. The polar aprotic solvent is selected from DMF, DMA, NMP and DMSO, preferably DMA. The alkali metal hydroxide is selected from LiOH, KOH and NaOH, preferably LiOH. The amount of alkali metal hydroxide is preferably between 1.8 and 2.5 molar equivalents with respect to 2,3-dichloroquinoxaline, preferably around 2 molar equivalents.
In a fifth embodiment, the first step of the process of the present invention provides compounds of Formulae (II) or (II′) in a crude purity higher than 70% at a temperature lower than 90° C., preferably, in crude purity higher than 70% at a temperature lower than 60° C. The reaction time is preferably between 5 to 24 hours, more preferably between 10 and 20 hours and even more preferably between 15 and 18 hours. The solvent is preferably an aprotic solvent selected from DMF, NMP, DMA, and DMSO, more preferably DMA. The alkali metal base is selected from LiOH, NaOH and KOH, preferably LiOH.
In a sixth embodiment, the alkali metal hydroxide is used in a molar ratio of 0.5 to 2.5 compared to 2,3-dichloroquinoxaline. Preferably, the alkyli metal hydroxide is used in a molar ratio of 0.8 to 1.5 compared to 2,3-dichloroquinoxaline, more preferably in a molar ratio of about 1.2.
In a seventh embodiment, the present invention relates to any compounds of Formulae (I) or (I′) obtained or obtainable by the process described herein.
In a height embodiment, the present invention relates to any compounds of Formulae (II) or (II′) obtained or obtainable by step a) of the process described herein.
1H NMR was recorded on 400 MHz spectrometers. Chemical shifts (6) are reported in ppm relative to the residual solvent signal (δ=2.49 ppm for 1H NMR in DMSO-d6). 1H NMR data are reported as follows: chemical shift (multiplicity, coupling constants, and number of hydrogens). Multiplicity is abbreviated as follows: s (singlet), d (doublet), t (triplet), q (quartet), m (multiplet), br (broad).
NMR, HPLC and MS data provided in the examples described below are registered on:
NMR: Bruker DPX-300, using residual signal of deuterated solvent as internal reference.
HPLC: Waters Alliance 2695, column Waters XBridge C8 3.5 μm 4.6×50 mm, conditions: solvent A (H2O with 0.1% TFA), solvent B (ACN with 0.05% TFA), gradient 5% B to 100% B over 8 min, UV detection with PDA Water 996 (230-400 nm).
LCMS method: 0.1% TFA in H2O, B: 0.1% TFA in ACN Flow Rate: 2.0 mL/min Column: Xbridge C8 (50×4.6 mm, 3.5μ).
UPLC/MS: Waters Acquity, column Waters Acquity UPLC BEH C18 1.7 μm 2.1×50 mm, conditions: solvent A (10 mM ammonium acetate in water+5% ACN), solvent B (ACN), gradient 5% B to 100% B over 3 min, UV detection (PDA, 230-400 nm) and MS detection (SQ detector, positive and negative ESI modes, cone voltage 30V).
In a 3 L three-necked round bottom flask containing a solution of 1-methyl-1H-imidazole-4-sulfonamide (80.98 g; 502.4 mmol; 1.0 eq.) in DMA (900 mL), lithium hydroxide (22.86 g; 954.6 mmol; 1.9 eq.) was added in one portion and after stirring for 8 minutes 2,3-dichloroquinoxaline (100 g; 502.4 mmol; 1.0 eq.) was added in one portion.
The reaction mixture was stirred at 50° C. for 16 h until completion (ca about 3% of 2,3-dichloroquinoxaline remaining and only about 1-2% of 3-chloroquinoxalin-2-ol formed as a side product, determined by UPLC/MS). The reaction mixture (yellow solution) was cooled down to 2° C. (ice-bath) and HCl (502.4 mL; 1N) was added drop wise over 40 minutes keeping temperature below 15° C.
Resulting pale yellow fine suspension was stirred for 5 minutes (T=13° C.) and was filtered through a glass filter. The resulting yellow off-white cake was sucked dry under vacuum for 2 h and was then washed twice with cold water (5° C.; 500 mL). The resulting white suspension was sucked dry for 10 minutes and was dried overnight at 40° C. under vacuum to give N-(3-chloroquinoxalin-2-yl)-1-methyl-1H-imidazole-4-sulfonamide (149.32 g, yield, 91.8%, 97% (AUC) by UPLC/MS; 0% of 3-chloroquinoxalin-2-ol; 3% of 2,3-dichloroquinoxaline and by NMR: 2.4% (w/w) of 1-methyl-1H-imidazole-4-sulfonamide as pale yellow powder.
In a 3 L three-necked round bottom flask containing a solution of 2-[(dimethylamino) methyl]-1-methyl-1H-imidazole-4-sulfonamide (109.67 g; 502.41 mmol; 1.0 eq.) in DMA (900.0 ml), lithium hydroxide (22.86 g; 954.6 mmol; 1.9 eq.) was added in one portion and after stiffing for 8 minutes 2,3-dichloroquinoxaline (100.0 g; 502.41 mmol; 1.0 eq.) was added in one portion. The reaction mixture was stirred at 50° C. for 16 h until completion (ca about 4% of 2,3-dichloroquinoxaline remaining and only 3% of 3-chloroquinoxalin-2-ol formed as a side product, determined by UPLC/MS)
Reaction mixture (brown solution) was cooled down to 5° C. (ice-bath) and HCl (502.4 mL; 1N) was added drop wise over 35 minutes keeping temperature below 17° C. The resulting beige fine suspension was stirred for 5 minutes (T=13° C.) and was filtered through a glass filter. The beige cake was sucked dry under vacuum for 10 minutes and was then washed twice with cold water (T=5° C.; V=2×500 mL; 2×5V). The resulting white suspension was sucked dry over weekend and was dried for 16 h at 40° C. under 30 mbar to give N-(3-chloroquinoxalin-2-yl)-2-[(dimethylamino)methyl]-1-methyl-1H-imidazole-4-sulfonamide [168.44 g, yield, 88%, 94% (AUC) by UPLC/MS; 1.25% of 3-chloroquinoxalin-2-ol; 3.4% of 2,3-dichloroquinoxaline and by NMR: 3.6% (w/w) of 2-[(dimethylamino)methyl]-1-methyl-1H-imidazole-4-sulfonamide as off-white powder.
In a 150 mL flask under nitrogen containing a solution of 4-fluorobenzenesulfonamide (4.40 g; 25.12 mmol; 1.0 eq.) in DMA (45.00 ml), lithium hydroxide (1.14 g; 47.73 mmol; 1.9 eq.) was added in one portion and after stiffing for 10 minutes 2,3-dichloroquinoxaline (5.00 g; 25.12 mmol; 1.0 eq.) was added in one portion. Reaction mixture was stirred at 50° C. for 20 h until completion as indicated by UPLC/MS The reaction mixture (yellow solution) was cooled down to 5° C. (ice-bath) and HCl (25.12 ml; 1N) was added in one pot and resulting suspension was aged in an ice bath for 20 minutes until complete precipitation. Then suspension was filtered and washed with water (3×50 mL), then resulting solid was washed with MTBE to remove 2, 3 dichloroquinoxaline in excess (2×30 mL). Additional crop was obtained upon precipitation in the MTBE phase (heptane was added to the filtrate to initiate precipitation and a second crop was obtained by filtration). The 2 crops were combined to give after drying title product as white powder (5.59 g; 65.9%).
HPLC Purity: 99.3% (max plot), Rt: 3.76 min; UPLC/MS: purity: 100% (max plot), Rt: 1.06 min
In a 150 mL flask under N2 containing a solution of 2-chlorobenzenesulphonamide (4.81 g; 25.1 mmol; 1.0 eq.) in DMA (45 mL), lithium hydroxide (1.14 g; 47.7 mmol; 1.9 eq.) was added in one portion and after stirring for 10 minutes 2,3-dichloroquinoxaline (5.0 g; 25.12 mmol; 1.0 eq.) was added in one portion. The reaction mixture was stirred at 50° C. for 20 h until completion as indicated by UPLC/MS.
The reaction mixture (clear brown solution) was then cooled down to 5° C. (ice-bath) and hydrochloric acid 1N (25.1 mL) was added in one pot. The resulting suspension was aged in a ice bath for 20 minutes until complete precipitation. Then, the suspension was filtered and washed with water (3×50 mL), and the resulting solid was washed with MTBE (2×30 mL) to remove 2, 3 dichloroquinoxaline in excess. Additional crop was obtained upon precipitation in the MTBE phase (heptane was added to the filtrate to initiate precipitation and a second crop was obtained by filtration). The 2 crops were combined to give after drying title product as beige solid (6.25 g; crude yield: 70.2%).
HPLC Purity: 98.9% (max plot), Rt: 3.86 min; UPLC/MS: purity 100% (max plot), Rt: 1.08 min
In 25 mL flask under N2 containing a solution of 2-chlorobenzenesulphonamide (0.48 g; 2.51 mmol; 1.0 eq.) in DMA (4.5 mL), potassium carbonate (0.66 g; 4.77 mmol; 1.9 eq.) was added in one portion and after stirring for 10 minutes 2,3-dichloroquinoxaline (500 mg; 2.51 mmol; 1.0 eq.) was added in one portion. The reaction mixture was stirred at 50° C. for 22 h until analysis by UPLC/MS. The reaction mixture (yellow solution) was then stirred at 100° C. for the weekend until analysis by UPLC/MS. The reaction mixture was then cooled down to 5° C. (ice-bath) and hydrochloric acid 1N (5.0 mL) was added in one pot and resulting suspension was filtered and washed with water then with MTBE to give after drying title product as beige solid (173 mg; crude yield: 19.4%). PLC/MS: purity: 100% (max plot), Rt: 1.08 min
The following further compounds may be obtained using the above set of protocols using lithium, potassium hydroxide or alkali metal hydroxide (Table 1).
The preferred conditions are the ones using lithium hydroxide in DMA at a temperature of about 50° C. Better isolated yields were obtained using lithium hydroxide over other bases, such as K2CO3 (Table 2).
In addition, when an alkali metal hydroxide is used, the purity profile of the crude reaction is improved (Table 3). The formation of the byproduct or impurity during the reaction minimized in these conditions as compared to the use of other bases such as K2CO3.
The purity profiles of the crude reaction depicted in Table 3 are determined by chromatography analysis with the following HPLC Method: Solvant A: 0.1% TFA in H2O, Solvent B: 0.1% TFA in ACN: Flow-2.0 mL/min. Column: Waters X Bridge C8 (50×4.6 mm, 3.50.
In particular, the formation of impurity or byproduct E during the reaction is minimized when LiOH is used as compared to other bases such as K2CO3. Removal of the impurity or byproduct E from the desired N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formula (II) often required extensive washing, crystallization or other purification procedures.
Other examples of bases for the reaction are exemplified in the table 4, illustrating the improved purity profile from the reaction mixture, and the use of lower reaction temperature to reach similar or better isolated yields (Table 4).
The synthesis of compounds of Formula (II′) is illustrated by the following example wherein A′ is reacted with B′. The crude ratio of compounds A′, B′ C′ and D′, in table 5, has been determined according to the method described above.
In a second step, the intermediate N-(3-chloro-quinoxalin-2-yl)-sulfonamides of formula (II) is converted to the N-(3-amino-quinoxalin-2-yl)-sulfonamides (I) by reaction with an amine of formula NH2R2 wherein R2 is as above defined (Scheme 1, Step 2) with a pyridine base, preferably 2,6-dimethylpyridine (lutidine). Preferably, the amount of the pyridine base i.e. lutidine, is between 0.5 and 2 molar equivalent compared to compounds of Formula (II), more preferably between 0.8 and 1.2 molar equivalents, more preferably around 1.1 molar equivalent.
200 mg of N-(3-chloroquinoxalin-2-yl)-1-methyl-1H-pyrazole-3-sulfonamide, 180 mg of 3-(2-amino-4,6-dimethoxyphenoxy)propan-1-ol and 72 μL of Lutidine were poured into 2 mL of propanol and heated at 140° C. under microwave irradiation (high absorption mode) for ca. 3 h until completion of reaction. The reaction mixture was cooled to RT, filtered and the collected product was washed with 1-propanol and then dried under vacuum. 251 mg of N-(3-{[2-(3-hydroxypropoxy)-3,5-dimethoxyphenyl]amino}quinoxalin-2-yl)-1-methyl-1H-pyrazole-3-sulfonamide was isolated as a light yellow powder (80%). MS-FAB (M+H+)=515.1.
In a 4 L three necked-flask under N2, containing N-(3-chloroquinoxalin-2-yl)-1-methyl-1H-imidazole-4-sulfonamide (100.0 g; 308.9 mmol; 1.0 eq.) and 3-(2-amino-4-methoxy-phenyl)-propan-1-ol (61.58 g; 339.8 mmol; 1.1 eq.) suspended in 1-butanol (2 L), 2,6-dimethylpyridine (39.44 mL; 339.8 mmol; 1.1 eq.) was added in one portion.
The reaction mixture was stirred at 120° C. (oil bath at 125° C.) under N2 for 42 h until completion of reaction.
The temperature was allowed to cool down to RT and the reaction mixture was filtered through a glass filter and resulting yellow cake was washed first twice with n-butanol (2×400 ml) then twice with distilled water (2×500 mL). After filtration and sucking dry for 30 minutes, 100% purity was achieved (determined by UPLC/MS). The product was dried under vacuum at 35° C. for 2 days until no weight variation was observed anymore to give N-(3-{[2-(3-hydroxypropyl)-5-methoxyphenyl]amino}quinoxalin-2-yl)-1-methyl-1H-imidazole-4-sulfonamide [115.69 g, yield: 79.9%, 98% (AUC) by HPLC; CHN: [C22H24N6O4S] Corrected: C56.40%, H5.16%, N17.94%;
Found: C56.30%, H5.12%, N17.86%; 0.1% Cl; <0.1% water; 0.3% n-butanol by NMR.]
Other examples of bases for the above reaction are exemplified in the table 6, illustrating the improved purity profile by the use of lutidine.
The following further compounds I-3 to I-93 may be obtained using the above set out protocols (Table 7), in particular using lutidine as a base.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10188170.4 | Oct 2010 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2011/068152 | 10/18/2011 | WO | 00 | 4/19/2013 |
| Number | Date | Country | |
|---|---|---|---|
| 61424933 | Dec 2010 | US |
